Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1800629
rs1800629
TNF
169 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2008 2008
dbSNP: rs1799983
rs1799983
246 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2018 2018
dbSNP: rs121913499
rs121913499
51 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.010 1.000 1 2013 2013
dbSNP: rs1549758
rs1549758
7 0.807 0.360 7 150998638 synonymous variant T/C snv 0.76 0.76 0.010 1.000 1 2018 2018
dbSNP: rs121913503
rs121913503
23 0.689 0.200 15 90088606 missense variant C/A;T snv 0.010 1.000 1 2013 2013
dbSNP: rs4704397
rs4704397
13 0.807 0.200 5 77222617 intron variant G/A snv 0.54 0.010 1.000 1 2015 2015
dbSNP: rs189261858
rs189261858
8 0.776 0.160 14 81143407 missense variant G/A;T snv 2.3E-04 0.010 1.000 1 2016 2016
dbSNP: rs732609
rs732609
TPO
5 0.827 0.160 2 1496155 missense variant A/C;G snv 0.43 0.010 1.000 1 2017 2017
dbSNP: rs2046045
rs2046045
4 0.925 0.080 5 77239986 intron variant T/C;G snv 0.010 1.000 1 2015 2015
dbSNP: rs6885099
rs6885099
4 1.000 0.040 5 77234524 intron variant A/G snv 0.52 0.010 1.000 1 2015 2015